LeishMANIAdb
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Major vault protein

Quick info Localization Expansion Sequence features Structure Putative motif mimicry Homologs Download

Quick info

Protein:
Major vault protein
Gene product:
major vault protein, putative
Species:
Leishmania major
UniProt:
MVP_LEIMA
TriTrypDb:
LmjF.05.0060 , LMJLV39_050005500 * , LMJSD75_050005500 *
Length:
833

Localization

Secreted promastigote
Source Evidence on protein Close homologs
Cuervo et al. no yes: 0
Hassani et al. no yes: 0
Forrest at al. (metacyclic) no yes: 0
Forrest at al. (procyclic) no yes: 0
Silverman et al. no yes: 0
Pissara et al. no yes: 0
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 9
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005634 nucleus 5 12
GO:0005737 cytoplasm 2 12
GO:0032991 protein-containing complex 1 12
GO:0043226 organelle 2 12
GO:0043227 membrane-bounded organelle 3 12
GO:0043229 intracellular organelle 3 12
GO:0043231 intracellular membrane-bounded organelle 4 12
GO:0110165 cellular anatomical entity 1 12
GO:1990904 ribonucleoprotein complex 2 12

Expansion

Sequence features

Q4QJJ7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QJJ7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 104 108 PF00656 0.572
CLV_C14_Caspase3-7 130 134 PF00656 0.453
CLV_C14_Caspase3-7 253 257 PF00656 0.491
CLV_MEL_PAP_1 510 516 PF00089 0.297
CLV_NRD_NRD_1 244 246 PF00675 0.411
CLV_NRD_NRD_1 303 305 PF00675 0.399
CLV_NRD_NRD_1 34 36 PF00675 0.410
CLV_NRD_NRD_1 374 376 PF00675 0.433
CLV_NRD_NRD_1 465 467 PF00675 0.306
CLV_PCSK_FUR_1 7 11 PF00082 0.393
CLV_PCSK_KEX2_1 244 246 PF00082 0.435
CLV_PCSK_KEX2_1 303 305 PF00082 0.415
CLV_PCSK_KEX2_1 347 349 PF00082 0.278
CLV_PCSK_KEX2_1 374 376 PF00082 0.434
CLV_PCSK_KEX2_1 775 777 PF00082 0.497
CLV_PCSK_KEX2_1 9 11 PF00082 0.420
CLV_PCSK_PC1ET2_1 347 349 PF00082 0.278
CLV_PCSK_PC1ET2_1 775 777 PF00082 0.549
CLV_PCSK_PC1ET2_1 9 11 PF00082 0.403
CLV_PCSK_SKI1_1 129 133 PF00082 0.314
CLV_PCSK_SKI1_1 234 238 PF00082 0.416
CLV_PCSK_SKI1_1 471 475 PF00082 0.228
CLV_PCSK_SKI1_1 744 748 PF00082 0.513
DEG_APCC_DBOX_1 356 364 PF00400 0.394
DEG_APCC_DBOX_1 782 790 PF00400 0.566
DEG_COP1_1 547 556 PF00400 0.514
DEG_ODPH_VHL_1 481 492 PF01847 0.489
DOC_CYCLIN_RxL_1 600 611 PF00134 0.514
DOC_CYCLIN_RxL_1 681 692 PF00134 0.492
DOC_CYCLIN_yCln2_LP_2 116 119 PF00134 0.478
DOC_MAPK_gen_1 106 116 PF00069 0.525
DOC_MAPK_gen_1 444 452 PF00069 0.354
DOC_MAPK_gen_1 466 474 PF00069 0.428
DOC_MAPK_gen_1 669 678 PF00069 0.460
DOC_MAPK_gen_1 7 16 PF00069 0.355
DOC_MAPK_gen_1 706 714 PF00069 0.432
DOC_MAPK_JIP1_4 401 407 PF00069 0.450
DOC_MAPK_MEF2A_6 466 474 PF00069 0.428
DOC_MAPK_MEF2A_6 635 643 PF00069 0.479
DOC_MAPK_MEF2A_6 708 716 PF00069 0.450
DOC_PP1_RVXF_1 446 453 PF00149 0.315
DOC_PP1_RVXF_1 601 608 PF00149 0.514
DOC_PP2B_LxvP_1 116 119 PF13499 0.478
DOC_PP4_FxxP_1 310 313 PF00568 0.369
DOC_PP4_FxxP_1 509 512 PF00568 0.453
DOC_PP4_FxxP_1 551 554 PF00568 0.428
DOC_SPAK_OSR1_1 451 455 PF12202 0.428
DOC_USP7_MATH_1 232 236 PF00917 0.480
DOC_USP7_MATH_1 273 277 PF00917 0.493
DOC_USP7_MATH_1 427 431 PF00917 0.548
DOC_USP7_MATH_1 47 51 PF00917 0.428
DOC_USP7_MATH_1 571 575 PF00917 0.488
DOC_USP7_UBL2_3 109 113 PF12436 0.509
DOC_USP7_UBL2_3 671 675 PF12436 0.452
DOC_WW_Pin1_4 423 428 PF00397 0.458
DOC_WW_Pin1_4 493 498 PF00397 0.479
DOC_WW_Pin1_4 813 818 PF00397 0.500
LIG_14-3-3_CanoR_1 229 236 PF00244 0.460
LIG_14-3-3_CanoR_1 513 521 PF00244 0.440
LIG_14-3-3_CanoR_1 530 536 PF00244 0.440
LIG_14-3-3_CanoR_1 549 554 PF00244 0.529
LIG_14-3-3_CanoR_1 582 588 PF00244 0.428
LIG_14-3-3_CanoR_1 606 614 PF00244 0.458
LIG_14-3-3_CanoR_1 731 738 PF00244 0.422
LIG_Actin_WH2_2 214 231 PF00022 0.493
LIG_APCC_ABBA_1 481 486 PF00400 0.514
LIG_BIR_II_1 1 5 PF00653 0.409
LIG_BRCT_BRCA1_1 573 577 PF00533 0.367
LIG_eIF4E_1 170 176 PF01652 0.533
LIG_FHA_1 22 28 PF00498 0.422
LIG_FHA_1 306 312 PF00498 0.502
LIG_FHA_1 390 396 PF00498 0.429
LIG_FHA_1 494 500 PF00498 0.506
LIG_FHA_1 516 522 PF00498 0.453
LIG_FHA_1 548 554 PF00498 0.514
LIG_FHA_1 681 687 PF00498 0.430
LIG_FHA_2 251 257 PF00498 0.470
LIG_FHA_2 32 38 PF00498 0.399
LIG_FHA_2 389 395 PF00498 0.469
LIG_FHA_2 606 612 PF00498 0.449
LIG_FHA_2 613 619 PF00498 0.409
LIG_GBD_Chelix_1 198 206 PF00786 0.333
LIG_LIR_Apic_2 308 313 PF02991 0.387
LIG_LIR_Apic_2 550 554 PF02991 0.514
LIG_LIR_Gen_1 235 240 PF02991 0.386
LIG_LIR_Gen_1 281 289 PF02991 0.388
LIG_LIR_Gen_1 485 492 PF02991 0.431
LIG_LIR_Gen_1 574 585 PF02991 0.441
LIG_LIR_Gen_1 683 690 PF02991 0.429
LIG_LIR_LC3C_4 322 327 PF02991 0.503
LIG_LIR_Nem_3 235 239 PF02991 0.403
LIG_LIR_Nem_3 281 285 PF02991 0.374
LIG_LIR_Nem_3 445 450 PF02991 0.502
LIG_LIR_Nem_3 485 490 PF02991 0.431
LIG_LIR_Nem_3 534 538 PF02991 0.471
LIG_LIR_Nem_3 574 580 PF02991 0.429
LIG_LIR_Nem_3 683 688 PF02991 0.433
LIG_LIR_Nem_3 93 98 PF02991 0.509
LIG_PTB_Apo_2 434 441 PF02174 0.484
LIG_SH2_CRK 11 15 PF00017 0.449
LIG_SH2_CRK 447 451 PF00017 0.428
LIG_SH2_CRK 56 60 PF00017 0.428
LIG_SH2_PTP2 13 16 PF00017 0.328
LIG_SH2_PTP2 282 285 PF00017 0.481
LIG_SH2_SRC 13 16 PF00017 0.385
LIG_SH2_SRC 282 285 PF00017 0.454
LIG_SH2_SRC 362 365 PF00017 0.514
LIG_SH2_STAP1 265 269 PF00017 0.439
LIG_SH2_STAT5 13 16 PF00017 0.328
LIG_SH2_STAT5 152 155 PF00017 0.453
LIG_SH2_STAT5 205 208 PF00017 0.462
LIG_SH2_STAT5 282 285 PF00017 0.350
LIG_SH2_STAT5 33 36 PF00017 0.207
LIG_SH2_STAT5 362 365 PF00017 0.440
LIG_SH2_STAT5 386 389 PF00017 0.422
LIG_SH2_STAT5 538 541 PF00017 0.469
LIG_SH2_STAT5 56 59 PF00017 0.428
LIG_SH2_STAT5 751 754 PF00017 0.503
LIG_SH2_STAT5 809 812 PF00017 0.496
LIG_SH3_3 143 149 PF00018 0.453
LIG_SH3_3 165 171 PF00018 0.366
LIG_SH3_3 353 359 PF00018 0.516
LIG_SH3_3 46 52 PF00018 0.298
LIG_SH3_3 470 476 PF00018 0.428
LIG_SH3_3 494 500 PF00018 0.451
LIG_SH3_3 56 62 PF00018 0.437
LIG_SH3_3 93 99 PF00018 0.430
LIG_SUMO_SIM_anti_2 157 163 PF11976 0.398
LIG_SUMO_SIM_anti_2 322 328 PF11976 0.463
LIG_SUMO_SIM_par_1 157 163 PF11976 0.433
LIG_SUMO_SIM_par_1 403 409 PF11976 0.533
LIG_SUMO_SIM_par_1 416 422 PF11976 0.489
LIG_SUMO_SIM_par_1 488 493 PF11976 0.456
LIG_SUMO_SIM_par_1 515 525 PF11976 0.453
LIG_SUMO_SIM_par_1 712 719 PF11976 0.446
LIG_SxIP_EBH_1 146 155 PF03271 0.533
LIG_TRAF2_1 208 211 PF00917 0.342
LIG_TRAF2_1 419 422 PF00917 0.514
LIG_TRAF2_1 483 486 PF00917 0.440
LIG_TRAF2_1 99 102 PF00917 0.494
LIG_TRFH_1 309 313 PF08558 0.365
LIG_TRFH_1 95 99 PF08558 0.281
LIG_UBA3_1 221 226 PF00899 0.510
LIG_UBA3_1 376 381 PF00899 0.389
LIG_UBA3_1 800 807 PF00899 0.480
LIG_WRC_WIRS_1 233 238 PF05994 0.452
LIG_WRC_WIRS_1 577 582 PF05994 0.281
LIG_WW_3 51 55 PF00397 0.315
MOD_CDK_SPK_2 493 498 PF00069 0.396
MOD_CK1_1 430 436 PF00069 0.561
MOD_CK1_1 493 499 PF00069 0.399
MOD_CK1_1 502 508 PF00069 0.347
MOD_CK1_1 515 521 PF00069 0.240
MOD_CK1_1 547 553 PF00069 0.428
MOD_CK1_1 622 628 PF00069 0.389
MOD_CK1_1 698 704 PF00069 0.470
MOD_CK2_1 205 211 PF00069 0.376
MOD_CK2_1 275 281 PF00069 0.382
MOD_CK2_1 31 37 PF00069 0.420
MOD_CK2_1 388 394 PF00069 0.338
MOD_CK2_1 439 445 PF00069 0.498
MOD_CK2_1 698 704 PF00069 0.470
MOD_Cter_Amidation 242 245 PF01082 0.348
MOD_GlcNHglycan 230 233 PF01048 0.478
MOD_GlcNHglycan 27 30 PF01048 0.511
MOD_GlcNHglycan 277 280 PF01048 0.441
MOD_GlcNHglycan 492 495 PF01048 0.281
MOD_GlcNHglycan 583 586 PF01048 0.297
MOD_GlcNHglycan 697 700 PF01048 0.441
MOD_GlcNHglycan 732 735 PF01048 0.487
MOD_GlcNHglycan 74 78 PF01048 0.326
MOD_GSK3_1 205 212 PF00069 0.426
MOD_GSK3_1 21 28 PF00069 0.512
MOD_GSK3_1 228 235 PF00069 0.427
MOD_GSK3_1 423 430 PF00069 0.537
MOD_GSK3_1 618 625 PF00069 0.332
MOD_GSK3_1 629 636 PF00069 0.472
MOD_GSK3_1 809 816 PF00069 0.499
MOD_N-GLC_1 18 23 PF02516 0.398
MOD_N-GLC_1 181 186 PF02516 0.358
MOD_N-GLC_1 388 393 PF02516 0.337
MOD_N-GLC_1 427 432 PF02516 0.549
MOD_NEK2_1 1 6 PF00069 0.554
MOD_NEK2_1 228 233 PF00069 0.430
MOD_NEK2_1 297 302 PF00069 0.542
MOD_NEK2_1 388 393 PF00069 0.315
MOD_NEK2_1 490 495 PF00069 0.315
MOD_NEK2_1 531 536 PF00069 0.282
MOD_NEK2_1 605 610 PF00069 0.290
MOD_NEK2_1 612 617 PF00069 0.270
MOD_NEK2_1 633 638 PF00069 0.475
MOD_NEK2_1 73 78 PF00069 0.428
MOD_NEK2_1 749 754 PF00069 0.484
MOD_NEK2_1 800 805 PF00069 0.581
MOD_NEK2_1 820 825 PF00069 0.306
MOD_NEK2_2 250 255 PF00069 0.509
MOD_NEK2_2 305 310 PF00069 0.397
MOD_PIKK_1 544 550 PF00454 0.311
MOD_PIKK_1 644 650 PF00454 0.479
MOD_PIKK_1 749 755 PF00454 0.540
MOD_PIKK_1 793 799 PF00454 0.561
MOD_PK_1 549 555 PF00069 0.297
MOD_PKA_2 228 234 PF00069 0.449
MOD_PKA_2 512 518 PF00069 0.297
MOD_PKA_2 531 537 PF00069 0.209
MOD_PKA_2 581 587 PF00069 0.281
MOD_PKA_2 605 611 PF00069 0.322
MOD_PKA_2 629 635 PF00069 0.478
MOD_PKA_2 730 736 PF00069 0.424
MOD_PKA_2 782 788 PF00069 0.475
MOD_Plk_1 209 215 PF00069 0.489
MOD_Plk_1 305 311 PF00069 0.394
MOD_Plk_1 485 491 PF00069 0.297
MOD_Plk_4 1 7 PF00069 0.550
MOD_Plk_4 148 154 PF00069 0.284
MOD_Plk_4 164 170 PF00069 0.245
MOD_Plk_4 209 215 PF00069 0.410
MOD_Plk_4 217 223 PF00069 0.394
MOD_Plk_4 297 303 PF00069 0.463
MOD_Plk_4 305 311 PF00069 0.357
MOD_Plk_4 515 521 PF00069 0.333
MOD_Plk_4 782 788 PF00069 0.456
MOD_ProDKin_1 423 429 PF00069 0.323
MOD_ProDKin_1 493 499 PF00069 0.351
MOD_ProDKin_1 813 819 PF00069 0.501
MOD_SUMO_for_1 690 693 PF00179 0.520
MOD_SUMO_rev_2 101 111 PF00179 0.481
MOD_SUMO_rev_2 157 167 PF00179 0.443
MOD_SUMO_rev_2 223 228 PF00179 0.480
MOD_SUMO_rev_2 263 270 PF00179 0.442
MOD_SUMO_rev_2 361 371 PF00179 0.503
MOD_SUMO_rev_2 621 629 PF00179 0.282
MOD_SUMO_rev_2 698 707 PF00179 0.431
TRG_DiLeu_BaEn_1 330 335 PF01217 0.368
TRG_DiLeu_BaEn_1 668 673 PF01217 0.464
TRG_DiLeu_BaEn_2 305 311 PF01217 0.378
TRG_DiLeu_BaEn_4 330 336 PF01217 0.428
TRG_DiLeu_BaEn_4 485 491 PF01217 0.315
TRG_ENDOCYTIC_2 11 14 PF00928 0.350
TRG_ENDOCYTIC_2 282 285 PF00928 0.347
TRG_ENDOCYTIC_2 447 450 PF00928 0.492
TRG_ENDOCYTIC_2 538 541 PF00928 0.338
TRG_ENDOCYTIC_2 56 59 PF00928 0.281
TRG_ER_diArg_1 302 304 PF00400 0.435
TRG_ER_diArg_1 374 376 PF00400 0.496
TRG_ER_diArg_1 528 531 PF00400 0.401
TRG_ER_diArg_1 725 728 PF00400 0.336
TRG_NES_CRM1_1 315 331 PF08389 0.438
TRG_NLS_MonoExtC_3 465 470 PF00514 0.348

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6Z8 Leptomonas seymouri 36% 92%
A0A0N1I3S9 Leptomonas seymouri 82% 100%
A0A0S4ISQ0 Bodo saltans 40% 97%
A0A0S4JL46 Bodo saltans 60% 99%
A0A1X0NXD4 Trypanosomatidae 40% 100%
A0A1X0P2V2 Trypanosomatidae 66% 100%
A0A1X0P8P2 Trypanosomatidae 37% 97%
A0A3S7WNY9 Leishmania donovani 98% 100%
A0A3S7XAQ4 Leishmania donovani 36% 95%
A0A422NIL8 Trypanosoma rangeli 40% 99%
A0A422NLE5 Trypanosoma rangeli 36% 97%
A0A422NYK3 Trypanosoma rangeli 65% 98%
A4H452 Leishmania braziliensis 91% 100%
A4HP51 Leishmania braziliensis 35% 95%
A4HSC9 Leishmania infantum 98% 100%
A4IDF8 Leishmania infantum 36% 95%
C9ZPY2 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 64% 100%
D0A1L3 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 39% 97%
D0A336 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 34% 97%
E9AIP9 Leishmania braziliensis 43% 100%
E9AKB0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 96% 100%
E9ASV9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 34% 95%
P34118 Dictyostelium discoideum 50% 99%
P54659 Dictyostelium discoideum 49% 98%
Q14764 Homo sapiens 50% 93%
Q3SYU9 Bos taurus 50% 94%
Q4CUM2 Trypanosoma cruzi (strain CL Brener) 66% 99%
Q4Q1N7 Leishmania major 36% 99%
Q4QJJ7 Leishmania major 100% 100%
Q57Z03 Trypanosoma brucei brucei (strain 927/4 GUTat10.1) 64% 99%
Q5EAJ7 Strongylocentrotus purpuratus 50% 97%
Q5R9N2 Pongo abelii 50% 93%
Q5ZMI4 Gallus gallus 50% 98%
Q62667 Rattus norvegicus 49% 97%
Q6P3L0 Danio rerio 48% 97%
Q6PF69 Xenopus laevis 48% 98%
Q90405 Diplobatis ommata 49% 98%
Q9DGM7 Ictalurus punctatus 48% 96%
Q9EQK5 Mus musculus 49% 97%
V5AUX6 Trypanosoma cruzi 66% 99%
V5B0K2 Trypanosoma cruzi 39% 97%
V5BPE1 Trypanosoma cruzi 35% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS